Investigation of the Interaction of Quartz with Hydrogen under Supply of Mechanical Energy (II) Investigation by IR Spectroscopy

Infrared investigations demonstrate a chemical interaction of quartz in hydrogen atmosphere during mechanical activation: By means of the SiH stretching band the number of formed SiH-groups is estimated as a function of the period of activation. of activation. This number is more than one order of magnitude less than the total number of adsorbed molecules.     

X-ray and X-ray photoelectron spectra of vanadium oxides

X-ray (XS) and X-ray photoelectron (XPS) spectra are reported for vanadium oxides. Because of the multivalent character of vanadium in the oxide system high quality measurements can be used for chemical shift investigation. Both inner level and valence band spectroscopy give information on the electronic structure and their systematic change with increasing oxidation state. The experimental results are discussed favourable in terms of molecular orbital theory (MO-theory). The complete set of XS and XPS data reported here for V-oxides allows the identification of unknown vanadium oxidation states too.     

A linear relativistic method for the calculation of band structure in transition metals with results for Au

With a linear relativistic method we calculated the band structure of gold. A comparison with the results of a RAPW calculation shows that the deviation is about 3%. The effort of computational time is for the linear method considerably smaller than for the RAPW method.     

X-ray determination of mean square amplitudes of lattice oscillations in compounds with ZnS structure

A general method of determination of the mean square amplitudes of lattice oscillations (MSA) for crystals with sphalerite structure is described and applied to InP. The linearity of suitable functions of the measured integral BRAGG intensities of sin² θ/λ² is used for the verification of the parameters selected for the correction of extinction and DTS. In this way the accuracy of the results is increased. The MSAs of the InP-sublattices are evaluated. According to theoretical expectations the MSAs of the P-sublattice are larger because of the greater contributions of optical phonons.     

Use of N-benzyl-2-naphthohydroxamic acid as a highly selective reagent for solvent extraction and spectrophotometric determination of vanadium(V)

N-Benzyl-2-naphthohydroxamic acid extracts vanadium(V) selectively and quantitatively into chloroform from 2-8.5M hydrochloric acid in the presence of Mo(VI), Zr(IV) and Ce(IV). The extraction takes place quickly and gives a stable reddish-violet extract which shows an absorption maximum at 505 nm with molar absorptivity of (5.34 +/- 0.05) x 10(3) 1.mole(-1).cm(-1). The optimum range for the determination is 2.2-7.4 ppm of vanadium(V) in the final solution. The method has been used for the determination of vanadium in steels.     

Preparation of 125I-Lanreotide and its biodistribution in murine model of melanoma

Lanreotide, a somatostatin analogue, was radioiodinated with ¹²⁵I to explore the possibility of using ¹²³I labeled lanreotide as a diagnostic radiopharmaceutical for tumors overexpressing somatostatin (SST) receptors. Radioiodination was carried out with ¹²⁵I using chloramine T as the oxidant. The labeling yield was >90%. Characterization of ¹²⁵I-Lanreotide was carried out by paper electrophoresis as well as HPLC. ¹²⁵I-Lanreotide was purified by chromatography using a C18 Sep-Pak column. Radiochemical purity of the purified ¹²⁵I-Lanreotide thus obtained was >99%. Significant tumor uptake of ¹²⁵I-Lanreotide was observed in C57BL/6 mice bearing melanoma.     

Crystal and molecular structure of (2–3-η-2-Butyne-1,4-diol)-bis-(triphenylphosphan)-nickel(O) Ni{[(C6H5)3P]2 (C4H6O2)}

The crystal and molecular structure of (2–3-η-2-Butyne-1,4-diol)-bis-(triphenylphosphan)-nickel(O) has been determined by X-ray structure analysis. It crystallizes in the tetragonal space group 14 with the cell parameters a = b = 22.277(3), and c = 15.118 (4) Å. The structure was solved by the heavy atom method and refined to R = 0.0716. The coordination geometry about the nickel atom is trigonal-planar. Each molecule is hydrogen bonded to two neighbours. The result is an eight-membered oxygen ring.